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Spectrum: Autism Research News

News Archive

June 2015

Leaky filter leads to motion perception problem in autism

by  /  30 June 2015

Children with autism detect certain kinds of motion better than their peers do, but don’t tune out distracting visuals.
 

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Diverse features found for autism-linked chromosome changes

by  /  29 June 2015

The first in-depth look at people with alterations in the 1q21.1 chromosomal region reveals a range of features, from problems with fine motor skills to autism.

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Protein webs tangle up neurons in autism-linked disorder

by  /  26 June 2015

Star-shaped brain cells called astrocytes weave a web of proteins that derails brain development in the autism-like Costello syndrome. The findings add to mounting evidence that brain cells other than neurons contribute to autism.

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Young women bear high risk of having children with autism

by  /  25 June 2015

Older women and men are at high risk of having a child with autism — and so are teenage girls and parents whose age differs by at least a decade, according to a multinational study of more than 5 million children.

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New technology gives voice to nonverbal people with autism

by  /  22 June 2015

A new service provides personalized voices for people who use speech-generating devices. The service, called VocaliD, could help the nearly 25 percent of children with autism who speak few to no words.

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Body clock genes may set pace for sleep issues in autism

by  /  19 June 2015

People with autism are twice as likely to carry alterations in genes that regulate the circadian clock, or the body’s sleep-wake cycle as those without the disorder. The findings may help explain why most children with autism have trouble with sleep.

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Common glitches in chromosomes can cause cognitive problems

by  /  18 June 2015

More than 10 percent of people carry deletions or duplications of DNA that diminish their intellectual capacity. The findings, based on a large study of an Estonian population, suggest that the bigger the mutation, the more severe a person’s cognitive deficits.

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Enzyme’s discovery points to new approach for fragile X

by  /  16 June 2015

Researchers have discovered an enzyme that lowers brain levels of FMRP, the protein missing in people with fragile X syndrome. Blocking the enzyme may ease fragile X symptoms in people with the disorder who have low levels of FMRP and mild symptoms.

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Cell skeleton breakdown may spur autism symptoms in mice

by  /  15 June 2015

An autism-linked mutation in the SHANK3 gene alters the protein skeleton of mouse neurons. Repairing the scaffold eases the animals’ social deficits.

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Large Swedish study casts doubt on autism ‘epidemic’

by  /  12 June 2015

Although increasing numbers of people are receiving an autism diagnosis, the proportion of the population with autism symptoms has remained steady. This finding, from a study of more than 1 million Swedish children, backs the theory that autism’s rise stems from greater awareness of the disorder.

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